Hypothermically Stored Adipose-Derived Mesenchymal Stromal Cell Alginate Bandages Facilitate Use of Paracrine Molecules for Corneal Wound Healing

Int J Mol Sci. 2020 Aug 14;21(16):5849. doi: 10.3390/ijms21165849.

Abstract

Adipose-derived mesenchymal stromal cells (Ad-MSCs) may alleviate corneal injury through the secretion of therapeutic factors delivered at the injury site. We aimed to investigate the therapeutic factors secreted from hypothermically stored, alginate-encapsulated Ad-MSCs' bandages in in vitro and in vivo corneal wounds. Ad-MSCs were encapsulated in 1.2% w/v alginate gels to form bandages and stored at 15 °C for 72 h before assessing cell viability and co-culture with corneal scratch wounds. Genes of interest, including HGF, TSG-6, and IGF were identified by qPCR and a human cytokine array kit used to profile the therapeutic factors secreted. In vivo, bandages were applied to adult male mice corneas following epithelial debridement. Bandages were shown to maintain Ad-MSCs viability during storage and able to indirectly improve corneal wound healing in vivo. Soluble protein concentration and paracrine factors such as TSG-6, HGF, IL-8, and MCP-1 release were greatest following hypothermic storage. In vivo, Ad-MSCs bandages-treated groups reduced immune cell infiltration when compared to untreated groups. In conclusion, bandages were shown to maintain Ad-MSCs ability to produce a cocktail of key therapeutic factors following storage and that these soluble factors can improve in vitro and in vivo corneal wound healing.

Keywords: adipose-derived stem cells; cornea; hypothermic storage; paracrine factors; sodium alginate; stem cells bandage; wound model.

MeSH terms

  • Alginates / pharmacology*
  • Animals
  • Biomarkers / metabolism
  • Cell Survival / drug effects
  • Cornea / drug effects
  • Cornea / pathology*
  • Gene Expression Regulation / drug effects
  • Humans
  • Mesenchymal Stem Cells / cytology*
  • Mice
  • Models, Biological
  • Paracrine Communication* / drug effects
  • Preservation, Biological*
  • Solubility
  • Stromal Cells / cytology
  • Stromal Cells / drug effects
  • Transcription, Genetic / drug effects
  • Wound Healing* / drug effects
  • Wound Healing* / genetics

Substances

  • Alginates
  • Biomarkers